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WO2006111296A3 - Formes galeniques et preparations combinees d'inhibiteur de la synthese de la pyrimidine pour l'obtention d'effets supplementaires sur le systeme immunitaire - Google Patents

Formes galeniques et preparations combinees d'inhibiteur de la synthese de la pyrimidine pour l'obtention d'effets supplementaires sur le systeme immunitaire Download PDF

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Publication number
WO2006111296A3
WO2006111296A3 PCT/EP2006/003291 EP2006003291W WO2006111296A3 WO 2006111296 A3 WO2006111296 A3 WO 2006111296A3 EP 2006003291 W EP2006003291 W EP 2006003291W WO 2006111296 A3 WO2006111296 A3 WO 2006111296A3
Authority
WO
WIPO (PCT)
Prior art keywords
dosage forms
immune system
biosynthesis inhibitors
additional effects
combined preparations
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2006/003291
Other languages
German (de)
English (en)
Other versions
WO2006111296A2 (fr
Inventor
Juergen Lindner
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of WO2006111296A2 publication Critical patent/WO2006111296A2/fr
Publication of WO2006111296A3 publication Critical patent/WO2006111296A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42—Oxazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4418—Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders

Landscapes

  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

L'invention concerne une préparation pharmaceutique, contenant au moins un inhibiteur de la synthèse de la pyrimidine, tel que la leflunomide. Selon l'invention, l'inhibiteur de la synthèse de la pyrimidine produit, après administration orale chez l'homme, en l'espace d'une heure une augmentation du taux de plasma sanguin de 1,1 mg/litre à 5 mg/litre.
PCT/EP2006/003291 2005-04-16 2006-04-11 Formes galeniques et preparations combinees d'inhibiteur de la synthese de la pyrimidine pour l'obtention d'effets supplementaires sur le systeme immunitaire Ceased WO2006111296A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102005017592.9 2005-04-16
DE102005017592A DE102005017592A1 (de) 2005-04-16 2005-04-16 Darreichungsformen und Kombinationspräparate von Pyrimidinbiosyntheseinhibitoren zur Erzielung zusätzlicher Wirkungen auf das Immunsystem

Publications (2)

Publication Number Publication Date
WO2006111296A2 WO2006111296A2 (fr) 2006-10-26
WO2006111296A3 true WO2006111296A3 (fr) 2007-04-19

Family

ID=36741320

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2006/003291 Ceased WO2006111296A2 (fr) 2005-04-16 2006-04-11 Formes galeniques et preparations combinees d'inhibiteur de la synthese de la pyrimidine pour l'obtention d'effets supplementaires sur le systeme immunitaire

Country Status (2)

Country Link
DE (1) DE102005017592A1 (fr)
WO (1) WO2006111296A2 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014096464A1 (fr) * 2013-01-31 2014-06-26 Alfred E. Tiefenbacher (Gmbh & Co. Kg) Composition pharmaceutique contenant du léflunomide
CN105473136A (zh) * 2013-04-18 2016-04-06 国家健康与医学研究院 用于在有此需要的受试者中抑制淋巴细胞增殖的方法和药物组合物

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0529500A1 (fr) * 1991-08-22 1993-03-03 Hoechst Aktiengesellschaft Médicament pour le traitement de réactions de rejet lors de transplantations d'organes
EP0538783A1 (fr) * 1991-10-23 1993-04-28 Hoechst Aktiengesellschaft Dérivés d'amides de l'acide n-phényl-cyano-2-hydroxy-3-crotonique et leur utilisation comme médicaments ayant des propriétés immunomodulants
EP0551230A1 (fr) * 1992-01-08 1993-07-14 Roussel Uclaf Dérivés 2-cyano 3-hydroxy énamides, leur procédé de préparation, leur application comme médicaments, les compositions pharmaceutiques les renfermant et les intermédiaires obtenus
DE19857009A1 (de) * 1998-12-10 2000-06-15 Aventis Pharma Gmbh Zubereitung mit verbesserter therapeutischer Breite, enthaltend Nukleotidsyntheseinhibitoren
WO2001043738A1 (fr) * 1999-12-15 2001-06-21 Aventis Pharma Deutschland Gmbh Procede de detection d'inhibiteurs de synthese nucleotidique ayant moins d'effets secondaires
US6294192B1 (en) * 1999-02-26 2001-09-25 Lipocine, Inc. Triglyceride-free compositions and methods for improved delivery of hydrophobic therapeutic agents
US20020022646A1 (en) * 2000-02-15 2002-02-21 Ilya Avrutov Method for systhesizing leflunomide
US20020077485A1 (en) * 2000-08-14 2002-06-20 Ilya Avrutov Micronized leflunomide

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0529500A1 (fr) * 1991-08-22 1993-03-03 Hoechst Aktiengesellschaft Médicament pour le traitement de réactions de rejet lors de transplantations d'organes
EP0538783A1 (fr) * 1991-10-23 1993-04-28 Hoechst Aktiengesellschaft Dérivés d'amides de l'acide n-phényl-cyano-2-hydroxy-3-crotonique et leur utilisation comme médicaments ayant des propriétés immunomodulants
EP0551230A1 (fr) * 1992-01-08 1993-07-14 Roussel Uclaf Dérivés 2-cyano 3-hydroxy énamides, leur procédé de préparation, leur application comme médicaments, les compositions pharmaceutiques les renfermant et les intermédiaires obtenus
DE19857009A1 (de) * 1998-12-10 2000-06-15 Aventis Pharma Gmbh Zubereitung mit verbesserter therapeutischer Breite, enthaltend Nukleotidsyntheseinhibitoren
US6294192B1 (en) * 1999-02-26 2001-09-25 Lipocine, Inc. Triglyceride-free compositions and methods for improved delivery of hydrophobic therapeutic agents
WO2001043738A1 (fr) * 1999-12-15 2001-06-21 Aventis Pharma Deutschland Gmbh Procede de detection d'inhibiteurs de synthese nucleotidique ayant moins d'effets secondaires
US20020022646A1 (en) * 2000-02-15 2002-02-21 Ilya Avrutov Method for systhesizing leflunomide
US20020077485A1 (en) * 2000-08-14 2002-06-20 Ilya Avrutov Micronized leflunomide

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
BRUSA PAOLA ET AL: "Pharmacokinetic monitoring of mycophenolate mofetil in kidney transplanted patients", FARMACO (LAUSANNE), vol. 55, no. 4, April 2000 (2000-04-01), pages 270 - 275, XP002407623, ISSN: 0014-827X *
DATABASE SCISEARCH [online] SUGIOKA N (REPRINT) ET AL: "Protein binding study of mycophenolate mofetil, a new immunosuppressant, in human plasma and pharmacokinetics in renal transplant patients", XP002407627, retrieved from STN Database accession no. 1997:584713 *
DIMITROVA PETYA ET AL: "Restriction of de novo pyrimidine biosynthesis inhibits Th1 cell activation and promotes Th2 cell differentiation", JOURNAL OF IMMUNOLOGY, vol. 169, no. 6, 15 September 2002 (2002-09-15), pages 3392 - 3399, XP002407624, ISSN: 0022-1767 *
JAPANESE JOURNAL OF TRANSPLANTATION, VOL. 32, NO. 1, PP. 33-42. ISSN: 0578-7947. PB - JAPANESE SOC TRANSPLANTATION, C/O DR KIKUO NOMOTO, NIHON GAKKAI JIMU CENTER, 5-16-9 HONKOMAGOME, BUNKYO-KU, TOKYO 131, JAPAN., 1997 *
LI JUN ET AL: "Pharmacokinetics of leflunomide in Chinese healthy volunteers", ACTA PHARMACOLOGICA SINICA, vol. 23, no. 6, June 2002 (2002-06-01), pages 551 - 555, XP002407622, ISSN: 1671-4083 *

Also Published As

Publication number Publication date
WO2006111296A2 (fr) 2006-10-26
DE102005017592A1 (de) 2006-10-19

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